DD141406A5 - Insektizide mittel - Google Patents

Insektizide mittel Download PDF

Info

Publication number: DD141406A5
Authority: DD; German Democratic Republic
Prior art keywords: spp; chloro; phenyl; fluoro; cblor
Prior art date: 1978-01-13

Application number

DD79210441A

Other languages

German (de)

English (en)

Inventor

Wilhelm Sirrenberg

Erich Klauke

Albrecht Marhold

Ingeborg Hammann

Wilhelm Stendel

Ingomar Krehan

Original Assignee

Bayer Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1978-01-13

Filing date

1979-01-11

Publication date

1980-04-30

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6029415&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DD141406(A5) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1979-01-11 Application filed by Bayer Ag filed Critical Bayer Ag

1980-04-30 Publication of DD141406A5 publication Critical patent/DD141406A5/de

Links

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239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
125000004789 chlorodifluoromethoxy group Chemical group ClC(O*)(F)F 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
230000036576 dermal application Effects 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
238000001035 drying Methods 0.000 description 1
244000078703 ectoparasite Species 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
230000012173 estrus Effects 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
238000001914 filtration Methods 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000006260 foam Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000000446 fuel Substances 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000003502 gasoline Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
238000002955 isolation Methods 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000004579 marble Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
SYBYTAAJFKOIEJ-UHFFFAOYSA-N methyl iso-propyl ketone Natural products CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
239000003595 mist Substances 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
VKKMPCPGXTUXTR-UHFFFAOYSA-N n-chloro-4-(trifluoromethoxy)aniline Chemical compound FC(F)(F)OC1=CC=C(NCl)C=C1 VKKMPCPGXTUXTR-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000003921 oil Substances 0.000 description 1
238000005457 optimization Methods 0.000 description 1
239000011368 organic material Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011435 rock Substances 0.000 description 1
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000779 smoke Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000004544 spot-on Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C265/00—Derivatives of isocyanic acid
- C07C265/16—Derivatives of isocyanic acid having isocyanate groups acylated
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C265/00—Derivatives of isocyanic acid
- C07C265/12—Derivatives of isocyanic acid having isocyanate groups bound to carbon atoms of six-membered aromatic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/48—Y being a hydrogen or a carbon atom
- C07C275/54—Y being a carbon atom of a six-membered aromatic ring, e.g. benzoylureas
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/39—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
- C07C323/43—Y being a hetero atom
- C07C323/44—X or Y being nitrogen atoms

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

DD79210441A 1978-01-13 1979-01-11 Insektizide mittel DD141406A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782801316 DE2801316A1 (de)	1978-01-13	1978-01-13	Substituierte n-phenyl-n'-(2-chlor- 6-fluor-benzoyl)-harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als insektizide

Publications (1)

Publication Number	Publication Date
DD141406A5 true DD141406A5 (de)	1980-04-30

Family

ID=6029415

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD79218771A DD148771A5 (de)	1978-01-13	1979-01-11	Verfahren zur herstellung von n-phenyl-n'-(2-chlor-6-fluorbenzoyl)-harnstoff
DD79210441A DD141406A5 (de)	1978-01-13	1979-01-11	Insektizide mittel

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
DD79218771A DD148771A5 (de)	1978-01-13	1979-01-11	Verfahren zur herstellung von n-phenyl-n'-(2-chlor-6-fluorbenzoyl)-harnstoff

Country Status (27)

Country	Link
US (1)	US4277499A (ro)
EP (1)	EP0003099B1 (ro)
JP (1)	JPS54100344A (ro)
AR (1)	AR223164A1 (ro)
AT (1)	AT363724B (ro)
AU (1)	AU518182B2 (ro)
BR (1)	BR7900196A (ro)
CA (1)	CA1095932A (ro)
CS (2)	CS205135B2 (ro)
DD (2)	DD148771A5 (ro)
DE (2)	DE2801316A1 (ro)
DK (1)	DK149448C (ro)
EG (1)	EG13734A (ro)
ES (1)	ES476796A1 (ro)
FI (1)	FI63392C (ro)
GR (1)	GR73087B (ro)
HU (1)	HU181405B (ro)
IL (1)	IL56405A (ro)
NO (1)	NO149386C (ro)
NZ (1)	NZ189349A (ro)
OA (1)	OA06146A (ro)
PH (1)	PH13875A (ro)
PL (2)	PL120284B1 (ro)
PT (1)	PT69039A (ro)
RO (1)	RO75588A (ro)
TR (1)	TR20429A (ro)
ZA (1)	ZA79145B (ro)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL160809C (nl) *	1970-05-15	1979-12-17	Duphar Int Res	Werkwijze ter bereiding van benzoylureumverbindingen, alsmede werkwijze ter bereiding van insekticide prepara- ten op basis van benzoylureumverbindingen.
US5245071A (en) *	1970-05-15	1993-09-14	Duphar International Research B.V.	Organic compounds derived from urea or thiourea
US5342958A (en) *	1970-05-15	1994-08-30	Solvay Duphar International Research B.V.	Organic compounds derived from urea or thiourea
USRE32418E (en) *	1977-05-13	1987-05-12	The Dow Chemical Company	Substituted(((phenyl)amino)carbonyl)-benzamides
DE2919292A1 (de) *	1979-05-12	1980-11-20	Bayer Ag	Substituierte harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als pflanzenbakterizide
EP0023884B1 (de) *	1979-07-11	1983-07-20	Ciba-Geigy Ag	N-Phenyl-N'-benzoylharnstoffe, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Mittel und ihre Verwendung zur Bekämpfung von Schädlingen
US4399152A (en) *	1980-04-03	1983-08-16	Duphar International B.V.	Substituted benzoyl ureas as insecticides
DK172687B1 (da) *	1981-07-30	1999-05-31	Dow Agrosciences Llc	Substituerede N-aroyl-N'-phenyl-urinstofforbindelser, mellemprodukt til brug ved fremstilling deraf, en fremgangsmåde til d
US4431667A (en) *	1981-12-04	1984-02-14	The Upjohn Company	Imino ethers useful for controlling insect and arachnoid pests
US4438110A (en)	1982-04-28	1984-03-20	Union Carbide Corporation	Chewing insect toxicant compositions
DE3217619A1 (de) *	1982-05-11	1983-11-17	Bayer Ag, 5090 Leverkusen	2,4-dihalogenbenzoyl-(thio)harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
DE3217620A1 (de) *	1982-05-11	1983-11-17	Bayer Ag, 5090 Leverkusen	2,5-dihalogenbenzoyl-(thio)harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
US4868215A (en) *	1982-07-26	1989-09-19	The Dow Chemical Company	Substituted N-aroyl N'-phenyl urea compounds
JPS6092260A (ja) *	1983-10-27	1985-05-23	Nippon Tokushu Noyaku Seizo Kk	新規アニリン誘導体
US4659736A (en) *	1984-01-21	1987-04-21	Bayer Aktiengesellschaft	Benzoyl urea compounds as agents for repelling snails and slugs
JPS60181063A (ja) *	1984-02-27	1985-09-14	Takeda Chem Ind Ltd	ベンゾイル尿素誘導体、その製造法及び殺虫剤
JPS60181067A (ja) *	1984-02-27	1985-09-14	Takeda Chem Ind Ltd	ベンゾイル尿素誘導体，その製造法及び殺虫剤
TR23048A (tr) *	1984-08-31	1989-02-14	Ciba Geigy Ag	Fenilbenzoiluereler,bunlarin im aline mahsus usul ve bunlarin zararhlarla muecadelede kullanimi
JPS6197255A (ja) *	1984-10-18	1986-05-15	チバ‐ガイギー　アクチエンゲゼルシヤフト	置換ｎ―ベンゾイル―ｎ’―２．５―ジクロロ―４―ヘキサフルオロプロピルオキシフェニル尿素、その製造方法及び該化合物を含有する組成物
DE3439364A1 (de) *	1984-10-27	1986-04-30	Bayer Ag, 5090 Leverkusen	Benzoylharnstoffe und zwischenprodukte
ES2038125T3 (es) *	1985-10-14	1993-07-16	Ciba-Geigy Ag	Benzoilfenilureas.
US5288756A (en) *	1985-10-14	1994-02-22	Ciba-Geigy Corporation	Benzoylphenylureas
DE3613062A1 (de) *	1986-04-18	1987-10-29	Hoechst Ag	N-benzoyl-n'-phenyl(thio)harnstoffe, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
GB8700838D0 (en) *	1987-01-15	1987-02-18	Shell Int Research	Termiticides
JP2661709B2 (ja) *	1988-07-08	1997-10-08	ダウ・ケミカル日本株式会社	高活性な農薬水和剤の製法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4013717A (en) *	1970-05-15	1977-03-22	U.S. Philips Corporation	Benzoyl phenyl urea derivatives having insecticidal activities
DE2531279C2 (de) *	1975-07-12	1983-07-14	Bayer Ag, 5090 Leverkusen	N-(3-Trifluormethyl-4-halogen-phenyl)- N'-benzoyl-harnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
DE2601780B2 (de) *	1976-01-20	1979-07-26	Bayer Ag, 5090 Leverkusen	N-Phenyl-N'-benzoylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
US4089975A (en) *	1977-05-13	1978-05-16	The Dow Chemical Company	Method of controlling manure-breeding insects
US4170657A (en) *	1977-05-13	1979-10-09	The Dow Chemical Company	Substituted(((phenyl)amino)carbonyl)-benzamides

1978
- 1978-01-13 DE DE19782801316 patent/DE2801316A1/de not_active Withdrawn
- 1978-12-29 NO NO784421A patent/NO149386C/no unknown
1979
- 1979-01-02 EP EP79100005A patent/EP0003099B1/de not_active Expired
- 1979-01-02 DE DE7979100005T patent/DE2960791D1/de not_active Expired
- 1979-01-05 PT PT69039A patent/PT69039A/pt unknown
- 1979-01-09 CS CS796220A patent/CS205135B2/cs unknown
- 1979-01-09 CS CS79203A patent/CS205134B2/cs unknown
- 1979-01-10 RO RO7996239A patent/RO75588A/ro unknown
- 1979-01-10 EG EG15/79A patent/EG13734A/xx active
- 1979-01-10 IL IL56405A patent/IL56405A/xx unknown
- 1979-01-10 NZ NZ189349A patent/NZ189349A/xx unknown
- 1979-01-11 TR TR20429A patent/TR20429A/xx unknown
- 1979-01-11 FI FI790087A patent/FI63392C/fi not_active IP Right Cessation
- 1979-01-11 DD DD79218771A patent/DD148771A5/de unknown
- 1979-01-11 DD DD79210441A patent/DD141406A5/de unknown
- 1979-01-11 JP JP105779A patent/JPS54100344A/ja active Granted
- 1979-01-12 BR BR7900196A patent/BR7900196A/pt unknown
- 1979-01-12 AT AT0023879A patent/AT363724B/de not_active IP Right Cessation
- 1979-01-12 HU HU79BA3747A patent/HU181405B/hu unknown
- 1979-01-12 GR GR58073A patent/GR73087B/el unknown
- 1979-01-12 ZA ZA79145A patent/ZA79145B/xx unknown
- 1979-01-12 PL PL1979219740A patent/PL120284B1/pl unknown
- 1979-01-12 ES ES476796A patent/ES476796A1/es not_active Expired
- 1979-01-12 DK DK13779A patent/DK149448C/da not_active IP Right Cessation
- 1979-01-12 AR AR275153A patent/AR223164A1/es active
- 1979-01-12 PH PH22058A patent/PH13875A/en unknown
- 1979-01-12 OA OA56705A patent/OA06146A/xx unknown
- 1979-01-12 PL PL1979212760A patent/PL116480B1/pl unknown
- 1979-01-12 CA CA319,597A patent/CA1095932A/en not_active Expired
- 1979-01-12 AU AU43340/79A patent/AU518182B2/en not_active Ceased
1980
- 1980-02-01 US US06/117,755 patent/US4277499A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
EP0003099A3 (en)	1979-08-22
NO149386C (no)	1984-04-11
JPS6123786B2 (ro)	1986-06-07
NO149386B (no)	1984-01-02
AT363724B (de)	1981-08-25
PH13875A (en)	1980-10-24
EP0003099A2 (de)	1979-07-25
EG13734A (en)	1982-06-30
AR223164A1 (es)	1981-07-31
NO784421L (no)	1979-07-16
AU4334079A (en)	1979-07-19
RO75588A (ro)	1981-01-30
PL120284B1 (en)	1982-02-27
GR73087B (ro)	1984-02-01
AU518182B2 (en)	1981-09-17
CA1095932A (en)	1981-02-17
ZA79145B (en)	1980-01-30
DK13779A (da)	1979-07-14
OA06146A (fr)	1981-06-30
CS205134B2 (en)	1981-04-30
DE2960791D1 (en)	1981-12-03
PL219740A1 (ro)	1980-11-17
DK149448B (da)	1986-06-16
PT69039A (pt)	1979-02-01
EP0003099B1 (de)	1981-09-16
PL116480B1 (en)	1981-06-30
DD148771A5 (de)	1981-06-10
ES476796A1 (es)	1979-06-01
TR20429A (tr)	1981-07-02
JPS54100344A (en)	1979-08-08
NZ189349A (en)	1981-03-16
FI790087A (fi)	1979-07-14
FI63392C (fi)	1983-06-10
US4277499A (en)	1981-07-07
ATA23879A (de)	1981-01-15
IL56405A0 (en)	1979-03-12
IL56405A (en)	1984-11-30
FI63392B (fi)	1983-02-28
CS205135B2 (en)	1981-04-30
HU181405B (en)	1983-07-28
DK149448C (da)	1986-11-24
DE2801316A1 (de)	1979-07-19
BR7900196A (pt)	1979-08-14
PL212760A1 (ro)	1980-04-21

Publication	Publication Date	Title
DE2601780C3 (ro)	1989-09-21
EP0003099B1 (de)	1981-09-16	Substituierte N-Phenyl-N'-(2-chlor-6-fluor-benzoyl)-harnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0093976B1 (de)	1986-09-10	2,4-Dihalogenbenzoyl-(thio)harnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
DE2504983C2 (de)	1982-10-21	Benzoylureido-nitro-diphenyläther, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0008435B1 (de)	1982-05-12	Substituierte N-Phenyl-N'-benzoyl-thioharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0093977A1 (de)	1983-11-16	2,5-Dihalogenbenzoyl-(thio)harnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
EP0009762B1 (de)	1981-08-05	Substituierte N-Benzoyl-N'-tert.-alkoxycarbonylphenyl-(thio)harnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
EP0042533B1 (de)	1984-03-14	Substituierte Benzoyl-(thio)harnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
DE2637947C2 (de)	1985-09-19	Tetrafluor-1,3-benzodioxanyl-benzoylharnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide
CH634303A5 (de)	1983-01-31	Phenylcarbamoyl-2-pyrazoline, verfahren zu deren herstellung sowie diese verbindungen enthaltende insektizide.
CH634304A5 (de)	1983-01-31	Phenylcarbamoyl-pyrazoline, verfahren zu deren herstellung sowie die verbindungen enthaltende insektizide.
EP0122449B1 (de)	1987-06-03	Benzoylharnstoffe
EP0123861B1 (de)	1988-04-20	Harnstoffderivate
DD209956A5 (de)	1984-05-30	Schaedlingsbekaempfungsmittel
DE2504982A1 (de)	1976-08-19	4-trifluormethyl-4'-benzoylureido- diphenylaether, verfahren zu ihrer herstellung und ihre verwendung als insektizide
EP0009103B1 (de)	1981-04-29	N-(O-Äthyl-S-n-propyl-(di)thiophosphoryloxy)-naphtalimide, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Schädlingsbekämpfungsmittel, ihre Herstellung und Verwendung
EP0005246A2 (de)	1979-11-14	Neues N-carboxyliertes Carbamat, Verfahren zu seiner Herstellung und seine insektizide Verwendung
EP0003766A1 (de)	1979-09-05	N-(omega-Chloralkanoyl)-N'-trifluormethylphenyl-harnstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung als Pflanzenschutzmittel
DE3640175A1 (de)	1988-06-01	Benzoyl(thio)harnstoffe
DE3932534A1 (de)	1991-04-11	Substituierte benzoylharnstoff-derivate
EP0172510A2 (de)	1986-02-26	Benzoylharnstoffe
EP0092757A1 (de)	1983-11-02	N-substituierte O-Pyrazol-4-yl-carbaminsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel
DE2504984A1 (de)	1976-08-19	Benzoylureido-diphenylaether, verfahren zu ihrer herstellung und ihre verwendung als insektizide